BEUDAMED
    11 results · 28ms · Sources: EU EUDAMED, US FDA

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    TC+ SYSTEM (TILTING C-ARM SYSTEM)

    FDA 510(k)
    FDA Class 2 ·Radiology

    GALAXY FIXATION SYSTEM

    FDA UDI
    ORTHOFIX SRL·18033509859465·ROD D 6 MM L 180 MM

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981203139·Interbody, 9mm x 36mm x 18mm, 0 deg

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981195144·Interbody, 9mm x 36mm x 18mm, 0 deg

    Galaxy Fixation System

    FDA UDI
    ORTHOFIX SRL·18033509859809·ROD D 6 MM L 180 MM STERILE

    BIOPSY CUP FORCEPS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CANNULATED CANCELLOUS SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GAMMA-CLONE ANTI-C (MONOCLONAL)

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·May 14, 2019

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·January 30, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·December 22, 2010

    C-TAPER COCR LFIT HEAD 36MM/0

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·July 15, 2014